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Quality Consultant to the Life Science industry

1 month ago

Copenhagen, Copenhagen, Denmark DAQUMA Full time
Quality Consultant to the Life Science industry

DAQUMA Copenhagen, Capital Region of Denmark, Denmark

In the summer of 2022, we started a consultancy supporting life science companies with IT implementations. We believe in a flexible and flat hierarchy where you can partake in directing DAQUMA's and your professional course.

DAQUMA is off to a great start, and therefore we are looking for more people to invite in. We seek to democratize the company and that is why we are not only seeking an employee, but someone who would like to take part in making decisions and have an impact on DAQUMA's journey.

About the role

As a Quality Consultant, you will contribute to delivering IT validation, IT process validation, and compliance services for our clients in the regulated life science industry. Your primary responsibilities will include assisting with the development of IT validation test plans, conducting assessments, and ensuring compliance with regulatory requirements. You'll work closely with senior consultants and client teams to contribute to high-impact projects while honing your skills.

At DAQUMA, we spend time and effort in team building, as our team is the most valuable to us. Therefore, we truly appreciate every single consultant, and we offer:

  • A competitive salary package.
  • A flexible social benefits package.
  • Exciting engagements to further your experience in the Life Science and Pharma industries.
  • A scale-up and engaging work culture, we hope that you would like to be part of.

Key Responsibilities

  • Develop and write IT test plans, focusing on IT requirements, IT process validation, and risk controls.
  • Assess and document validation processes to meet client and regulatory expectations.
  • Collaborate with clients to design and implement validation frameworks for IT systems, including processes critical to regulatory compliance.
  • Leverage tools such as eTIMS for creating and linking requirements and test plans.
  • Support cross-functional teams to ensure timely and accurate project delivery.

What We're Looking For

We imagine you to:

  • Have 2-5 years of experience in IT validation, IT process validation, or similar roles within the life science industry or another regulated sector.
  • Possess knowledge of IT requirements, risk controls, and how to test and document them.
  • Be familiar with validation tools like eTIMS or equivalent systems.
  • Understand regulatory frameworks such as GxP and IT compliance standards.
  • Demonstrate strong organizational and communication skills to work effectively with clients and teams.
  • Be adaptable and proactive, thriving in a fast-paced consultancy environment.
  • Preferred: Experience in GMP validation processes and working in international settings.

Formalities

If you want to join this exciting new adventure and help our clients reach their goals, then upload your CV directly on LinkedIn.

If you have questions call Mads on the number +45 6146 8041.

We will be reviewing applications as they come.

Find us on LinkedIn or our website.

Seniority level

Mid-Senior level

Employment type

Full-time

Industries

IT Services and IT Consulting

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